OpenAlex Citation Counts

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OpenAlex is a bibliographic catalogue of scientific papers, authors and institutions accessible in open access mode, named after the Library of Alexandria. It's citation coverage is excellent and I hope you will find utility in this listing of citing articles!

If you click the article title, you'll navigate to the article, as listed in CrossRef. If you click the Open Access links, you'll navigate to the "best Open Access location". Clicking the citation count will open this listing for that article. Lastly at the bottom of the page, you'll find basic pagination options.

Requested Article:

Systematic differences in discovery of genetic effects on gene expression and complex traits
Hakhamanesh Mostafavi, Jeffrey P. Spence, Sahin Naqvi, et al.
Nature Genetics (2023) Vol. 55, Iss. 11, pp. 1866-1875
Closed Access | Times Cited: 155

Showing 1-25 of 155 citing articles:

Bayesian estimation of gene constraint from an evolutionary model with gene features
Tony Zeng, Jeffrey P. Spence, Hakhamanesh Mostafavi, et al.
Nature Genetics (2024) Vol. 56, Iss. 8, pp. 1632-1643
Open Access | Times Cited: 26

Massively parallel characterization of regulatory elements in the developing human cortex
Chengyu Deng, Sean Whalen, Marilyn Steyert, et al.
Science (2024) Vol. 384, Iss. 6698
Closed Access | Times Cited: 23

Cell-type-specific and disease-associated expression quantitative trait loci in the human lung
Heini M. Natri, Christina B. Azodi, Lance Peter, et al.
Nature Genetics (2024) Vol. 56, Iss. 4, pp. 595-604
Open Access | Times Cited: 22

Sources of gene expression variation in a globally diverse human cohort
Dylan J. Taylor, Surya B. Chhetri, Michael G. Tassia, et al.
Nature (2024) Vol. 632, Iss. 8023, pp. 122-130
Open Access | Times Cited: 19

Non-linear transcriptional responses to gradual modulation of transcription factor dosage
Júlia Domingo, Mariia Minaeva, John Morris, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 12

Single-cell RNA sequencing of human tissue supports successful drug targets
Emma Dann, Erin Teeple, Rasa Elmentaite, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 10

Epigenomic insights into common human disease pathology
Christopher G. Bell
Cellular and Molecular Life Sciences (2024) Vol. 81, Iss. 1
Open Access | Times Cited: 10

Adipose tissue eQTL meta-analysis highlights the contribution of allelic heterogeneity to gene expression regulation and cardiometabolic traits
Sarah M. Brotman, Julia S. El-Sayed Moustafa, Li Guan, et al.
Nature Genetics (2025)
Closed Access | Times Cited: 1

Integration of functional genomics and statistical fine-mapping systematically characterizes adult-onset and childhood-onset asthma genetic associations.
Xiaoyuan Zhong, Robert D. Mitchell, Christine Billstrand, et al.
medRxiv (Cold Spring Harbor Laboratory) (2025)
Open Access | Times Cited: 1

Multiomic QTL mapping reveals phenotypic complexity of GWAS loci and prioritizes putative causal variants
Timothy D. Arthur, Jennifer Nguyen, Benjamin A. Henson, et al.
Cell Genomics (2025), pp. 100775-100775
Open Access | Times Cited: 1

Transfer learning reveals sequence determinants of the quantitative response to transcription factor dosage
Sahin Naqvi, Seungsoo Kim, Saman Tabatabaee, et al.
Cell Genomics (2025), pp. 100780-100780
Open Access | Times Cited: 1

Macroevolutionary divergence of gene expression driven by selection on protein abundance
Alexander L. Cope, Joshua G. Schraiber, Matthew W. Pennell
Science (2025) Vol. 387, Iss. 6738, pp. 1063-1068
Closed Access | Times Cited: 1

Spatially resolved mapping of cells associated with human complex traits
Liyang Song, Wenhao Chen, Junren Hou, et al.
Nature (2025)
Open Access | Times Cited: 1

Systemic lupus erythematosus genetics: insights into pathogenesis and implications for therapy
Yogita Ghodke‐Puranik, Mikhail Olferiev, Mary K. Crow
Nature Reviews Rheumatology (2024) Vol. 20, Iss. 10, pp. 635-648
Closed Access | Times Cited: 8

Integrating leiomyoma genetics, epigenomics, and single-cell transcriptomics reveals causal genetic variants, genes, and cell types
Kadir Buyukcelebi, Alexander James Duval, Fatih Abdula, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 6

Social-Science Genomics: Progress, Challenges, and Future Directions
Daniel J. Benjamin, David Cesarini, Patrick Turley, et al.
(2024)
Open Access | Times Cited: 6

Variants in tubule epithelial regulatory elements mediate most heritable differences in human kidney function
Gabriel B. Loeb, Pooja Kathail, Richard W. Shuai, et al.
Nature Genetics (2024) Vol. 56, Iss. 10, pp. 2078-2092
Closed Access | Times Cited: 6

Exponential family measurement error models for single-cell CRISPR screens
Timothy Barry, Kathryn Roeder, Eugene Katsevich
Biostatistics (2024) Vol. 25, Iss. 4, pp. 1254-1272
Open Access | Times Cited: 5

A Novel Macrophage Subpopulation Conveys Increased Genetic Risk of Coronary Artery Disease
Jiahao Jiang, Thomas K. Hiron, Thomas A. Agbaedeng, et al.
Circulation Research (2024) Vol. 135, Iss. 1, pp. 6-25
Open Access | Times Cited: 5

Conditional frequency spectra as a tool for studying selection on complex traits in biobanks
Roshni Patel, Clemens L. Weiß, Huisheng Zhu, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 5

Unlocking gene regulation with sequence-to-function models
Alexander Sasse, Maria Chikina, Sara Mostafavi
Nature Methods (2024) Vol. 21, Iss. 8, pp. 1374-1377
Closed Access | Times Cited: 5

Bayesian estimation of gene constraint from an evolutionary model with gene features
Tony Zeng, Jeffrey P. Spence, Hakhamanesh Mostafavi, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 11

Osteoarthritis as an Enhanceropathy: Gene Regulation in Complex Musculoskeletal Disease
Jack B. Roberts, Sarah J. Rice
Current Rheumatology Reports (2024) Vol. 26, Iss. 6, pp. 222-234
Open Access | Times Cited: 4

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